Clinical Trials Reporting Program

• Will I have access to data from my submissions?
• Will it be shared with grantees or others outside of NCI?

Will I have access to data from my submissions?
Yes. In response to requests from users, NCI is developing reporting systems to allow submitting organizations to use CTRP for their own clinical research portfolio management.

Will it be shared with grantees or others outside of NCI?
Protocol documents, IRB approval, Informed Consent forms, and Trial Summary Reports will not be shared with anyone other than the submitter.

Once a trial has been successfully registered with CTRP, the initial set of data elements supplied by the submitter when registering the trial, can be viewed by all CTRP users who have a valid user account.

Trial data elements abstracted by NCI's CTRO that correspond to clinicaltrials.gov data elements may be shared to the same extent they are on clinicaltrials.gov.